A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626607



Internal ID6666757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62451001..62451528hg38UCSC Ensembl
Innerchr11:62451001..62451528hg38UCSC Ensembl
Outerchr11:62450615..62451963hg38UCSC Ensembl
chr11:62218473..62219000hg19UCSC Ensembl
Innerchr11:62218473..62219000hg19UCSC Ensembl
Outerchr11:62218087..62219435hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14179617, essv14179674, essv14179665, essv14179680, essv14179634, essv14179626, essv14179666, essv14179629, essv14179663, essv14179650, essv14179689, essv14179695, essv14179661, essv14179647, essv14179694, essv14179639, essv14179693, essv14179624, essv14179631, essv14179620, essv14179690, essv14179623, essv14179619, essv14179632, essv14179678, essv14179656, essv14179679, essv14179668, essv14179646, essv14179658, essv14179699, essv14179697, essv14179657, essv14179659, essv14179642, essv14179636, essv14179688, essv14179649, essv14179673, essv14179685, essv14179628, essv14179640, essv14179669, essv14179687, essv14179627, essv14179621, essv14179651, essv14179618, essv14179622, essv14179675, essv14179662, essv14179660, essv14179684, essv14179667, essv14179671, essv14179635, essv14179644, essv14179664, essv14179676, essv14179643, essv14179655, essv14179691, essv14179672, essv14179648, essv14179637, essv14179653, essv14179681, essv14179630, essv14179652, essv14179686, essv14179641, essv14179683, essv14179670, essv14179625, essv14179645, essv14179654, essv14179692, essv14179633, essv14179682, essv14179696, essv14179638, essv14179677, essv14179698
SamplesHG00356, HG01603, HG01130, HG01302, HG00234, HG01519, NA12286, HG00328, NA20535, HG00155, HG00160, NA20775, HG01403, HG01082, HG01537, HG01182, HG01131, HG01680, HG01204, NA12287, HG01551, HG00256, NA20532, HG03667, NA20761, NA20505, NA12843, NA12282, NA12004, HG02233, NA20504, HG01061, HG01272, HG00121, NA20754, HG01124, HG00141, NA12761, NA19908, HG00149, HG00150, NA19774, HG00125, HG00258, HG02220, NA19658, HG01362, HG00114, HG00306, HG00159, HG02304, HG00108, NA20512, HG01121, HG01670, HG01069, NA11892, HG00277, HG02111, NA20828, HG00101, NA20766, HG02690, HG00120, HG02345, NA20534, NA20756, HG02235, NA12812, NA20507, HG00379, HG01619, HG00320, NA20528, NA12874, HG01522, NA06994, HG00271, HG00107, HG00126, NA20339, HG01536, HG00128
Known GenesAHNAK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626607
Frequency
Sample Size2504
Observed Gain0
Observed Loss83
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer